Malignant soft tissue lesions Flashcards

1
Q

Most important factor for limiting recurrence

A

margins

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2
Q

Soft tissue sarcomas that spread to regional lymph nodes

A

rhabdomyosarcoma, synovial sarcoma, clear cell sarcoma, epitheloid sarcoma, angiosarcoma

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3
Q

Most common sarcoma in lower extremities, young adult, cystic appearing with fluid levels, may have mineralization

A

Synovial sarcoma, mets to lung, Surgical excision and radiation

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4
Q

Translocation for synovial sarcoma

A

X:18, SYT SSX1 or 2 fusion protein

vimentin, keratin, EMA

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5
Q

Aggressive soft tissue lesion, often in retroperitoneum but moth eaten apearance to metaphysis of long bone, histo blunt cigar shaped nuclei with pink cytoplast

A

Leiomyosarcoma

wide excision and radiation chemo if lung mets

desmin/actin (muscle), +vimentin (sarcoma)

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6
Q

old person, chronic venous statis, overlying skin changes

A

angiosarcoma, tumor from endothelium of blood vessels

surgery and radiation

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7
Q

young adult with tumor in hand or forearm, nodular pattern with central necrosis, eosinophilic cytoplasm

A

epitheliod sarcoma, keratin +, wide resection and radiation

beware of lymph node spread

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8
Q

20-40 yo, usually associated with tendons on dorsum of foot, sheets of cells with clear cytoplasma and spindle cells

A

clear cell sarcoma, amputation and chemo

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9
Q

clear cell sarcoma translocation and staining

A

S-100, HMB-45

t(12;22) EWS AFT1, neuroectodermal

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10
Q

most common soft tissue sarcoma in children

A

rhabdomyosarcoma

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11
Q

Translocation for rhabdomyosarcoma

A

t(2:13) Pax3-FKHR

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12
Q

Treatment for rhabdomyosarcoma

A

chemo, resection, radiation

Lymph node spread common, must do bone marrow aspiration

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13
Q

Stains positive in rhabdomyosarcoma

A

vitemin, desmin/actin, myosin(MyoD1)

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14
Q

most common soft tissue sarcoma, middle aged, deep lesions in thigh or retroperitoneum

A

Liposarcoma

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15
Q

chromosomal translocation of myxoid liposarcoma

A

t(12;16) CHOP,TLS

MDM2

always order CT chest/ab/pelvis in myxoid

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16
Q

Types of liposarcoma

A

well-differentieated, myxoid, round cell, pleomorphic, undiff

17
Q

treatment for liposarcoma

A

resection and radiation

18
Q

Important prognostic factor in melanoma

19
Q

Treatment of melanoma

A

<1mm local resection

> 1mm local resection with 1-2cm margin, sentinel node bx

20
Q

Tumor of brown fat

21
Q

Treatment of atypical liposarcoma

22
Q

Patient with history of abdominal wall cancer, possible historyof FAP or Gardner syndrome, aggressive bubbly lesion if in bone

A

Desmoid tumor (fibromatosis), desmoplastic fibroma

usually around shoulder

dense spindlecellsin rows with elongated nuclei

23
Q

Treatment of desmoid tumor

A

NSAID, chemo, resection

tamoxifen if estrogen receptor positive

increased beta catenin (trisomy 8 or 20)

24
Q

Recurrent atraumatic hemoarthrosis, possible erosive changes on xrays, blooms on MRI

A

PVNS (tenosynovial giant cell)

hemosiderin in giant cells

focal nodular (simpe excision), extensive synovectomy plus radiation otherwise

Over expression of CSF-1 (pexidantinib)

25
Middle aged patient with painful mass on finger tip, bluish color, nail ridging, sensitive
Glomus tumor (pain, tenderness, cold intolerance) - perivascular temp regulating structure small round blue cells on histo Marginal excision
26
Middle aged patient with metaplastic changes in synovial tissue and chondroid loose bodies in the joint
Synovial chondromatosis (osteochondromatosis if mineralized on xray) marbles in joint, histo shows hyaline cartilage remove loose bodes and synovectomy